Variant #0000561266 (NC_000017.10:g.38251324T>C, NM_001190918.1:c.*1689T>C (THRA))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.38251324T>C
DNA change (hg38) g.40095071T>C
Published as NR1D1(NM_021724.4):c.1298A>G (p.(Gln433Arg))
ISCN -
DB-ID THRA_000009
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THRA NM_001190918.1 ?/. - c.*1689T>C r.(=) p.(=)
NR1D1 NM_021724.3 ?/. - c.1298A>G r.(?) p.(Gln433Arg)


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